ClinVar Miner

List of variants in gene FAT4 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Gene type:
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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_001291303.3(FAT4):c.11820A>G (p.Ser3940=) rs17009721 0.02714
NM_001291303.3(FAT4):c.12852C>T (p.Ser4284=) rs17009819 0.02466
NM_001291303.3(FAT4):c.11488A>G (p.Lys3830Glu) rs17009684 0.02342
NM_001291303.3(FAT4):c.14183G>A (p.Arg4728Lys) rs72675395 0.01656
NM_001291303.3(FAT4):c.1101A>G (p.Val367=) rs57692448 0.01498
NM_001291303.3(FAT4):c.14135C>G (p.Ser4712Cys) rs147662558 0.01304
NM_001291303.3(FAT4):c.9876G>A (p.Gly3292=) rs115219562 0.01168
NM_001291303.3(FAT4):c.8842A>G (p.Ile2948Val) rs76048257 0.01112
NM_001291303.3(FAT4):c.13605G>A (p.Lys4535=) rs75469760 0.01048
NM_001291303.3(FAT4):c.8544C>T (p.Ser2848=) rs139132509 0.00802
NM_001291303.3(FAT4):c.11429A>G (p.His3810Arg) rs114637892 0.00732
NM_001291303.3(FAT4):c.12071G>A (p.Arg4024Gln) rs28515675 0.00726
NM_001291303.3(FAT4):c.4154T>C (p.Leu1385Ser) rs139883132 0.00597
NM_001291303.3(FAT4):c.10853C>T (p.Thr3618Met) rs111423173 0.00407
NM_001291303.3(FAT4):c.12855T>C (p.Asp4285=) rs78040862 0.00365
NM_001291303.3(FAT4):c.12070C>T (p.Arg4024Trp) rs138019311 0.00333
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val) rs142747281 0.00288
NM_001291303.3(FAT4):c.10390A>G (p.Ile3464Val) rs147872710 0.00237
NM_001291303.3(FAT4):c.1128G>A (p.Val376=) rs202216461 0.00236
NM_001291303.3(FAT4):c.524G>T (p.Arg175Leu) rs143534324 0.00217
NM_001291303.3(FAT4):c.5921-14C>T rs190218898 0.00151
NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val) rs145639192 0.00145
NM_001291303.3(FAT4):c.8021A>T (p.Asp2674Val) rs138655269 0.00121
NM_001291303.3(FAT4):c.11619C>T (p.Cys3873=) rs141328606 0.00092
NM_001291303.3(FAT4):c.3682C>G (p.Gln1228Glu) rs200227715 0.00087
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys) rs139716832 0.00061
NM_001291303.3(FAT4):c.12769G>A (p.Glu4257Lys) rs143513466 0.00056
NM_001291303.3(FAT4):c.11380C>T (p.Arg3794Trp) rs201859188 0.00020
NM_001291303.3(FAT4):c.1099G>A (p.Val367Ile) rs747531733 0.00013
NM_001291303.3(FAT4):c.10750C>G (p.Leu3584Val) rs751277769 0.00006
NM_001291303.3(FAT4):c.11906-17A>C rs748245015 0.00006
NM_001291303.3(FAT4):c.9800A>G (p.His3267Arg) rs773545119 0.00002
NM_001291303.3(FAT4):c.10247G>C (p.Ser3416Thr)
NM_001291303.3(FAT4):c.4195C>A (p.Pro1399Thr) rs1486226093
NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr) rs191329848

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